Evidence map›Paper›PMID 25219359›Full record

ArticleScientific reports2014

Regulation of T cell proliferation by JMJD6 and PDGF-BB during chronic hepatitis B infection.

Cai-Feng Chen, Xia Feng, Hui-Yu Liao, Wen-Jing Jin, Jian Zhang, Yu Wang, Lu-Lu Gong, Jing-Jun Liu, Xiao-Hui Yuan, Bin-Bin Zhao and 6 more

Open access · goldAbstract readComparative Study
In one paragraph

Article in Scientific reports, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
3.0field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

30 citing papers in PubMed, 43 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. [Immune status of inactive HBsAg antigen carriers with chronic HBV infection].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2024
    Article
  6. Review
  7. Review
  8. Article
  9. JMJD family proteins in cancer and inflammation.Signal transduction and targeted therapy · 2022
    Review
  10. Widespread hydroxylation of unstructured lysine-rich protein domains by JMJD6.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors at 5 institutions in 2 countries.

Cai-Feng Chen1] MOH Key Laboratory of Systems Biology of Pathogens, Institute of Pathogen Biology, Chinese Academy of Medical Sciences &Peking Union Medical College, Beijing, People's Republic of China [2].
Xia Feng1] Center for Infection and Immunity, YouAn Hospital, The Beijing Capital Medical University, Beijing, China [2].
Hui-Yu Liao1] Center for Infection and Immunity, YouAn Hospital, The Beijing Capital Medical University, Beijing, China [2].
Wen-Jing JinMOH Key Laboratory of Systems Biology of Pathogens, Institute of Pathogen Biology, Chinese Academy of Medical Sciences &Peking Union Medical College, Beijing, People's Republic of China.
Jian ZhangDiagnosis and Treatment Center of Liver Fibrosis, 302 Hospital, Beijing, China.
Yu WangDepartment of Immunology, Duke University Medical Center, Durham, NC 27710.
Lu-Lu GongMOH Key Laboratory of Systems Biology of Pathogens, Institute of Pathogen Biology, Chinese Academy of Medical Sciences &Peking Union Medical College, Beijing, People's Republic of China.
Jing-Jun LiuMOH Key Laboratory of Systems Biology of Pathogens, Institute of Pathogen Biology, Chinese Academy of Medical Sciences &Peking Union Medical College, Beijing, People's Republic of China.
Xiao-Hui YuanMOH Key Laboratory of Systems Biology of Pathogens, Institute of Pathogen Biology, Chinese Academy of Medical Sciences &Peking Union Medical College, Beijing, People's Republic of China.
Bin-Bin ZhaoMOH Key Laboratory of Systems Biology of Pathogens, Institute of Pathogen Biology, Chinese Academy of Medical Sciences &Peking Union Medical College, Beijing, People's Republic of China.
Ding ZhangMOH Key Laboratory of Systems Biology of Pathogens, Institute of Pathogen Biology, Chinese Academy of Medical Sciences &Peking Union Medical College, Beijing, People's Republic of China.
Guo-Feng ChenDiagnosis and Treatment Center of Liver Fibrosis, 302 Hospital, Beijing, China.
Ying WanBiomedical Analysis Center, The Third Military Medical University, Chongqing, China.
Jian GuoDepartment of Immunology, Duke University Medical Center, Durham, NC 27710.
Hui-Ping YanCenter for Infection and Immunity, YouAn Hospital, The Beijing Capital Medical University, Beijing, China.
You-Wen HeDepartment of Immunology, Duke University Medical Center, Durham, NC 27710.
302 Military Hospital of China · CNDuke Medical Center · USArmy Medical University · CNCapital Medical University · CNDuke University Hospital · US

Funding

BcI-2 family in T lymphocyte homeostasisR01AI074754 · NIAID · DUKE UNIVERSITY · PI HE, YOU-WEN · 2009 to 2013
$1.9M
NIAID NIH HHS AI074754NIAID NIH HHS R01 AI074754
6 · The paper itself

Abstract

T cell functional exhaustion during chronic hepatitis B virus (HBV) infection may contribute to the failed viral clearance; however, the underlying molecular mechanisms remain largely unknown. Here we demonstrate that jumonji domain-containing protein 6 (JMJD6) is a potential regulator of T cell proliferation during chronic HBV infection. The expression of JMJD6 was reduced in T lymphocytes in chronic hepatitis B (CHB) patients, and this reduction in JMJD6 expression was associated with impaired T cell proliferation. Moreover, silencing JMJD6 expression in primary human T cells impaired T cell proliferation. We found that JMJD6 promotes T cell proliferation by suppressing the mRNA expression of CDKN3. Furthermore, we have identified platelet derived growth factor-BB (PDGF-BB) as a regulator of JMJD6 expression. PDGF-BB downregulates JMJD6 expression and inhibits the proliferation of human primary T cells. Importantly, the expression levels of JMJD6 and PDGF-BB in lymphocytes from CHB patients were correlated with the degree of liver damage and the outcome of chronic HBV infection treatment. Our results demonstrate that PDGF-BB and JMJD6 regulate T cell function during chronic HBV infection and may provide insights for the treatment strategies for CHB patients.

Indexed as

Gene Expression RegulationAntiviral AgentsBecaplerminBlotting, WesternCase-Control StudiesCell ProliferationCells, CulturedCyclin-Dependent Kinase Inhibitor ProteinsDual-Specificity PhosphatasesHepatitis B, ChronicHepatitis B virusHumansJumonji Domain-Containing Histone DemethylasesLymphocyte ActivationProto-Oncogene Proteins c-sisReal-Time Polymerase Chain ReactionAntiviral AgentsBecaplerminCDKN3 protein, humanCyclin-Dependent Kinase Inhibitor ProteinsDual-Specificity PhosphatasesJMJD6 protein, humanJumonji Domain-Containing Histone DemethylasesProto-Oncogene Proteins c-sisRNA, Messenger

Identifiers

PMID25219359
PMCPMC4163673
OpenAlexW2042696406

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.